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  • 1
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 157-163 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Dynamic mechanical properties have been investigated for interpenetrating-network systems based on polyol-cured polyurethanes (PU) and 2 to 1 n-butyl acrylate-n-butyl methacrylate (Ac) networks. The systems were formed simultaneously (SIN) from all of the precursors and reactants for both networks in the same vessel, and sequentially (SIPN) by swelling a precured PU with the reactants that will form the Ac network. If the Ac network is formed after gelation of the PU, the IPNs are transparent and appear to have single T (tan δmax) between those of the homonetworks; visible-phase separation occurs if the Ac is intentionally polymerized prior to PU gelation. Damping curves were lower and broader and the T (tan δmax) and rubber moduli were higher for the SIN than for the SIPN systems. Up to 65 percent Ac, the T (tan δmax) data for both SIN and SIPN fit the Gordon-Taylor equation if a T (tan δmax) for the Ac homonetwork 7°C higher than observed is used, suggesting a higher crosslink density for the Ac network under these conditions. The differences in properties of the SIN and SIPN are assumed to be dependent on sample homogeneity and upon the presence of a tin catalyst in the SIN preparation. This can result in limited Ac-network formation and consequent phase separation before PU gelation has occurred, and the catalyst may also increase the extent of interaction, such as grafting or hydrogen-bond formation between the networks.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 6 (1960), S. 611-614 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The low-pressure compressibilities of acetonitrile, acetaldehyde, and their mixtures were measured in the temperature range 40° to 100°C. From these data second virial coefficients were determined for the pure components and for the mixture. The absolute value of the coefficient B12, characteristic of interaction between dissimilar molecules, was considerably larger than that for B11 or B22, which are characteristic of interactions between similar molecules. As a result it was not possible to predict the properties of the mixture with only data for the pure components. Calculations based on the Stockmayer potential and with conventional mixing rules gave seriously incorrect results for the second virial coefficient B12.The data were interpreted with the aid of an association theory. Dimerization equilibrium constants and enthalpies and entropies of formation were computed for the pure-component dimers and for the complex. The heat of formation for the complex was significantly larger than that for the dimers; comparison with energy terms calculated from electrostatic theory suggest that the structure of the complex is different from that of the pure-component dimers.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 735-740 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of NOx-air irradiations, with trace amounts of propane and propene present to monitor OH radical concentrations, have been carried out in a 5800-L evacuable environmental chamber to investigate radical levels and sources during such irradiations. The data obtained show conclusively that unknown radical sources are present, and that photolysis of initial nitrous acid can be, at best, only a minor source of radicals after ∼30-60 min of irradiation.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 14 (1982), S. 1071-1103 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: While environmental chamber data have been widely used to generate and validate computer models of the chemistry occurring in polluted atmospheres, the effects of the chambers on the gas-phase chemistry being studied have been poorly characterized. In order to investigate such chamber effects, a series of NOx - air irradiations, with trace levels of organics present to monitor OH radical concentrations, have been carried out in four different environmental chambers (ranging in volume from ∼100 to 40,000 L) at varying temperatures, humidities, pressures, and reaction conditions. In addition, a number of control experiments have been carried out to validate the technique for measuring OH radical levels in these irradiations. The data show that unknown sources of OH radicals are present in all of the chambers studied. The data are consistent with the presence of two distinct radical sources: (1) the photolysis of initially present HONO, whose importance increases with increasing NO2/NO concentration ratios, but which is a minor contributor to the overall radical flux after 30-60 min of irradiation, and (2) a constant (for these NOx - air irradiations) radical source which dominates beyond approximately the first 60 min of irradiation. The radical input rates, after the first ∽30-60 min of irradiation, are independent of the NO concentration, increase with increasing temperature, humidity, and NO2 concentration, are proportional to light intensity, and are dependent on the chamber employed. Although the exact nature of this radical source is still undetermined, results of experiments reported here allow a number of possible mechanisms to be ruled, out, and these are discussed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 14 (1982), S. 813-814 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 14 (1982), S. 781-788 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Relative rate constants for the reaction of OH radicals with a series of n-alkanes have been determined at 299 ± 2 K, using methyl nitrite photolysis in air as a source of OH radicals. Using a rate constant for the reaction of OH radicals with n-butane of 2.58 × 10-12 cm3 molecule-1s-1, the rate constants obtained are (X1012 cm3 molecule-1 s-1): propane 1.22 ± 0.05, n-pentane 4.13 ± 0.08, n-heptane 7.30 ± 0.17, n-octane 9.01 ± 0.19, n-nonane 10.7 ± 0.4, and n-decane 11.4 ± 0.6. The data for propane, n-pentane, and n-octane are in good agreement with literature values, while those for n-heptane, n-nonane, and n-decane are reported for the first time. These data show that the rate constant per secondary C - H bond is ∽40% higher for  - CH2 -  groups bonded to two other  - CH2 -  groups than for those bonded to a  - CH2 -  group and a  - CH3 group.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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